烷基
热稳定性
化学
RNA干扰
干扰(通信)
组合化学
药物化学
立体化学
生物信息学
计算机科学
有机化学
生物化学
核糖核酸
生物
电信
基因
频道(广播)
作者
Avijit Sahoo,Shalini Gupta,Gourav Das,Atanu Ghosh,Siddharam Shivappa Bagale,Surajit Sinha,Kiran R. Gore
标识
DOI:10.1021/acsmedchemlett.4c00140
摘要
Herein, we have demonstrated that the siRNA activity could be enhanced by incorporating the guide strand in the RISC complex through thermodynamic asymmetry caused by m3U-based destabilizing modifications. A nuclease stability study revealed that 2'-OMe-m3U and 2'-OEt-m3U modifications slightly improved the half-lives of siRNA strands in human serum. In the in vitro gene silencing assay, 2'-OMe-m3U modification at the 3'-overhang and cleavage site of the passenger strand in anti-renilla and anti-Bcl-2 siRNA duplexes were well-tolerated and exhibited improved gene silencing activity. However, gene silencing activity was attenuated when these modifications were incorporated at position 3 in the seed region of the antisense strand. The molecular modeling studies using these modifications at the seed region with the MID domain of hAGO2 explained that the 2'-alkoxy group makes steric interactions with the amino acid residues of the hAGO2 protein.
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